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Showing items 96-120 of 419 (17 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-11-15T07:48:36Z	Prognostic factors of unknown primary head and neck squamous cell carcinoma	Huang C.-C; Tseng F.-Y; Yeh T.-H; Wen Y.-H; Hsu C.-J; JENG-YUH KO; Lou P.-J; Chen Y.-S.
臺大學術典藏	2021-11-15T07:48:27Z	Postoperative intensity-modulated radiotherapy for squamous cell carcinoma of the external auditory canal and middle ear: Treatment outcomes, marginal misses, and perspective on target delineation	Chen W.-Y; Kuo S.-H; Chen Y.-H; Lu S.-H; Tsai C.-L; Chia-Hsien Cheng J; Hong R.-L; Chen Y.-F; Hsu C.-J; Lin K.-N; JENG-YUH KO; Lou P.-J; Wang C.-P; Chong F.-C; Wang C.-W.
臺大學術典藏	2021-10-14T03:38:52Z	Study on Wetting Properties of Periodical Nanopatterns by a Combinative Technique of Photolithography and Laser Lithography	Yang, Y. L.; Hsu, C. J.; Chang, T. L.; Kuo, L. S.; Chen, Ping-Hei; PING-HEI CHEN
臺大學術典藏	2021-08-18T07:39:54Z	Cognition and evolution of movement disorders of FOXG1-related syndrome	Wong L.-C.; Wu Y.-T.; Hsu C.-J.; Weng W.-C.; WEN-CHE TSAI; Lee W.-T.
臺大學術典藏	2021-08-18T07:39:50Z	Dietary intake and growth deficits in Rett syndrome—A cross-section study	Wong L.C.; Chen Y.-T.; Tsai S.-M.; Lin Y.-J.; Hsu C.-J.; Wang H.-P.; Hu S.-C.; Shen H.-Y.; WEN-CHE TSAI; Lee W.-T.
臺大學術典藏	2021-08-05T02:41:21Z	A novel synthesis of sulfurized magnetic biochar for aqueous Hg(II) capture as a potential method for environmental remediation in water	Hsu C.-J;Cheng Y.-H;Huang Y.-P;Atkinson J.D;Hsi H.-C.; Hsu C.-J; Cheng Y.-H; Huang Y.-P; Atkinson J.D; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏	2021-08-05T02:41:20Z	Adsorption of aqueous Hg2+ and inhibition of Hg0 re-emission from actual seawater flue gas desulfurization wastewater by using sulfurized activated carbon and NaClO	Hsu C.-J;Chen Y.-H;Hsi H.-C.; Hsu C.-J; Chen Y.-H; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏	2021-08-05T02:41:20Z	A simulation study of mercury immobilization in estuary sediment microcosm by activated carbon/clay-based thin-layer capping under artificial flow and turbation	Ting Y;Ch'ng B.-L;Chen C;Ou M.-Y;Cheng Y.-H;Hsu C.-J;Hsi H.-C.; Ting Y; Ch'ng B.-L; Chen C; Ou M.-Y; Cheng Y.-H; Hsu C.-J; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏	2021-07-26T10:01:32Z	A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss	Lin Y.-H;Lin Y.-H;Lu Y.-C;Liu T.-C;Chen C.-Y;Hsu C.-J;Chen P.-L;Wu C.-C.; Lin Y.-H; Lin Y.-H; Lu Y.-C; Liu T.-C; Chen C.-Y; Hsu C.-J; Chen P.-L; Wu C.-C.; CHIEN-YU CHEN
臺大學術典藏	2021-07-06T02:04:15Z	Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment	Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:11Z	Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing	Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:09Z	Identifying children with poor cochlear implantation outcomes using massively parallel sequencing	Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏	2021-07-06T02:04:02Z	A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss	Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:02Z	Prediction Model for Audiological Outcomes in Patients with GJB2 Mutations	Chen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Hsu C.-J.
臺大學術典藏	2021-07-06T02:03:57Z	Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct	Lin Y.-H.;Wu C.-C.;Lin Y.-H.;Lu Y.-C.;Chen C.-S.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Lin Y.-H.; Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.
臺大學術典藏	2021-07-06T02:03:57Z	Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations	Erdenechuluun J.; Lin Y.-H.; Ganbat K.; Bataakhuu D.; Makhbal Z.; Tsai C.-Y.; Lin Y.-H.; Chan Y.-H.; Hsu C.-J.; Hsu W.-C.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:03:53Z	Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population	Wu C.-C.;Tsai C.-Y.;Lin Y.-H.;Chen P.-Y.;Lin P.-H.;Cheng Y.-F.;Wu C.-M.;Lin Y.-H.;Lee C.-Y.;Erdenechuluun J.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Wu C.-C.; Tsai C.-Y.; Lin Y.-H.; Chen P.-Y.; Lin P.-H.; Cheng Y.-F.; Wu C.-M.; Lin Y.-H.; Lee C.-Y.; Erdenechuluun J.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.
臺大學術典藏	2021-07-06T02:03:49Z	An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response	Lin P.-H.; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Yang S.-Y.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Liu T.-C.
臺大學術典藏	2021-07-03T03:35:26Z	Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations	Wu C.-C.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏	2021-07-03T03:35:25Z	Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: A unique spectrum of mutations in Taiwan, including a frequent founder mutation	Wu C.-C.; Yeh T.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏	2021-07-03T03:35:23Z	Common clinical features of children with enlarged vestibular aqueduct and mondini dysplasia	Wu C.-C.; Chen Y.-S.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏	2021-07-03T03:35:08Z	Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families	Wu C.-C.; Chiu Y.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏	2021-07-03T03:35:03Z	Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children	Wu C.-C.; Lee Y.-C.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏	2021-07-03T03:35:01Z	Prospective mutation screening of three common deafness genes in a large Taiwanese cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities	Wu C.-C.; PEI-JER CHEN; Chiu Y.-H.; Lu Y.-C.; Wu M.-C.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:55Z	Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment	Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Liu A.Y.-Z.; Hwu W.-L.; Hsu C.-J.

Showing items 96-120 of 419 (17 Page(s) Totally)
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